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CRO Services.

Introduction:


PDC is a Full Service Contract Research Organization Headquartered in KSA dedicated to providing Clinical Research Solutions covering MENA Region through a Full spectrum of Clinical Research Services from Feasibility till Publication Support.
PDC partners with an elite portfolio of clients including multinational pharmaceutical corporations to identify therapeutic trends, streamline the investigation of drugs, devices and diagnostics, monitor clinical use and economic value, and control development costs by accelerating time to market in today’s competitive environment.
PDC conducts cutting edge clinical research solutions in a broad range of therapeutic areas.
Consider PDC to meet your clinical research goals, if you’re looking for a welcoming culture with high degree of expertise, integrity, and passion for clinical research.

PDC’s experienced Clinical Operations team is here to support your program’s needs. From study start-up to the study close out meetings, PDC’s experienced surely can help you maximize project performance, collect high-quality data, and to help ensure product safety and subjects rights

At PDC, we believe that constant communication with our clients is the key to our success. PDC works closely with clients to identify and implement solutions to support needs tailored per each clinical study project, even when priorities change during the project.to fulfil the triad of Project Management process
• Performance Quality – Ensuring that all steps of each study are completed with high quality results
• Adherence to Timelines – ensuring that all project timelines are met to keep the project within the assigned parameters in coordination with our sponsors
• Framed to Budget – assisting our clients to ensure that the study is completed within budget and avoid unnecessary extra costs

Our experienced CRAs, Clinical Project Managers and Clinical Project Leads offers comprehensive clinical monitoring services from feasibility through site closeout to support clinical trials in KSA, GCC and over MENA Region. Our clinical services are tailored to your needs, complimenting product development plans and overarching corporate and quality management policies. All monitoring activities are conducted in accordance with the study protocol, clinical monitoring plan, standard operating procedures, ICH GCP, and applicable local and regional regulations.
Our team covers all Study Monitoring aspects for clinical studies from Feasibility, Site Initiation visits, Interim Monitoring visits and Close Out visits along with Site Management support for Subjects Recruitment, Site supplies and Site team training

PDC provides regulatory consulting either as a customized stand-alone service or through our full service clinical trials. The deep regulatory knowledge of our professionals enables Our regulatory team ensure client satisfaction through focused procedures that ensures rapid achievement of tasks towards faster start up, closure and in compliance with applicable guidelines in KSA, GCC and over MENA region

Our Team of experienced Medical Writers are capable of producing high quality Clinical Study documents including
• Study protocols
• Investigator brochures
• Informed consent documents
• Safety update reports
• Medical publications
• Interim and fully integrated final clinical study report

PDC provides full spectrum of solutions Data Management for your clinical projects with ensured Quality data through all project phases utilizing top notched applications and high standard platforms for EDC
– Develop Data Management Plan
– Develop, Program & Test Validation Checks
– Database Setup
– Program Customised Listings
– Data Cleaning and Query Generation/Resolution
– Perform Data Coding
– Database Close Out
– Archive Database

Through Our Experienced Biostatisticians PDC provides full bio-statistical support and expertise in all aspects of clinical trials. PDC’s Statisticians are capable of analysis and presentation of clinical data using advanced and up to date statistical methodologies including SAS, our services ranges from protocol design to dissemination of results across all therapeutic areas.

Clinical Outsourcing and Partnering is one of our core businesses. Through our qualified personnel and from our pool of talented recruits

Capturing economic value of new pharmaceutical products, medical devices and other health technologies is becoming an essential part of product development and marketing

Setting up compassionate Drug use programs; procure and import drugs on behalf of patients or providers; and coordinate the delivery of the drugs across borders in MENA region

Join our team. Send your CV

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